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Updated: Feb 17, 2026
![Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F62334.jpg&w=3840&q=50)
Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
Published on: February 17, 2022
[IgE-κ type multiple myeloma achieving complete response with novel agents]
Tomomi Takei1, Tadao Ishida1, Masahiro Ikeda1
1Department of Hematology, Japanese Red Cross Medical Center.
IgE multiple myeloma (MM) is rare and aggressive. Early treatment with novel agents and autologous stem-cell transplantation (ASCT) offers improved survival for IgE MM patients.
Area of Science:
- Hematology
- Oncology
Background:
- IgE multiple myeloma (MM) is a rare subtype with a typically poor prognosis.
- Novel agents have improved outcomes in general MM, but data for IgE MM are limited.
Observation:
- A case of IgE-kappa MM in a 53-year-old male presenting with rib pain.
Findings:
- The patient received upfront multidrug chemotherapy including bortezomib and lenalidomide, followed by autologous stem-cell transplantation (ASCT).
- Complete response was achieved after subsequent treatment with pomalidomide.
- Previous reports indicate poor prognosis for refractory IgE MM treated with novel agents, contrasting with this patient's outcome.
Implications:
- Early use of novel agents and ASCT may significantly improve long-term survival in IgE MM.
- This case suggests a potential therapeutic strategy for improving outcomes in this rare MM subtype.
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